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1.
Physical and chemical analyses of distal tephra from the 1912 eruption of Novarupta, Alaska, show considerable variations in glass and mineral compositions. A combination of a 150°C range in temperature deduced from iron-titanium oxide geothermometry, and curved patterns in bivariant element plots of glass compositions indicate that a chamber of compositionally zoned magma existed prior to the eruption. Magma-mixing cannot explain these features. The magma chamber may have resembled the model recently proposed by McBirney (1980). A highly silicic, quartz-phyric magma with mean phenocryst compositions of An25 plagioclase, Fs42 orthopyroxene, at a temperature of 880°C and a water pressure of 1.4 kbar, was located above a more mafic, hotter magma, bearing phenocrysts of An45 plagioclase and Fs35, orthopyroxene.Our results on distal tephras compare favorably with those from a recently completed study at source by Hildreth (1983), suggesting that useful petrologic information about distant volcanoes can be obtained from both types of deposits. Compositionally heterogeneous abyssal tephra layers are common in the Gulf of Alaska. Eruptions from chambers of zoned magma may account for many of these layers.  相似文献   

2.
The Mt Somers Volcanics are part of a suite of mid-Cretaceous (89 ± 2 Ma) intermediate to silicic volcanics, erupted onto an eroded surface of Torlesse sediments. Rock types vary from basaltic andesite to high-silica rhyolite. Andesites are medium- to high-K with phenocrysts of plagioclase, orthopyroxene and pigeonite. Dacites are peraluminous and commonly contain granulite facies xenoliths and garnet xenocrysts. Equilibrium mineral assemblages indicate metamorphic pressures of close to 6 kbar at 800°C. Rhyolites are peraluminous with phenocrysts of quartz, sanidine, plagioclase, biotite, garnet and orthopyroxene. The ferromagnesian phases show textural evidence of magmatic crystallization and are chemically distinct from xenocryst phases in dacites. Equilibrium assemblages indicate that early magmatic crystallization occurred at close to 7 kbar (20 km depth) at above 850°C, with melt-water contents of less than 3.5%. Major-element contents, trace-element contents and an initial 87Sr/86Sr ratio of 0.7085 indicate that the rhyolites formed by partial melting of dominantly quartzo-feldspathic Torlesse sediments, leaving a granulite-facies residue. The chemical variation displayed by the rhyolites is best explained by fractional crystallization of the observed high-pressure phenocryst assemblage. Most elements show a compositional gap between rhyolite and dacite. The major-element, trace-element and Sr isotope compositions of the intermediate lavas are best explained by assimilation of lower crustal material combined with fractional crystallization in mantle-derived tholeiitic magmas. Magmatism was the result of heat and magma flux from the mantle, during the change from compressive to extensional tectonics after the culmination of the Rangitata Orogeny.  相似文献   

3.
The Moshirabad pluton is located southwest of the Sanandaj–Sirjan Metamorphic Belt, Qorveh, western Iran. The pluton is composed of diorite, monzodiorite, quartz diorite, quartz monzodiorite, tonalite, granodiorite, granite, aplite, and pegmatite. In this study 31 samples from various rocks were chosen for whole‐rock analyses and 15 samples from different lithologies were chosen for mineral chemical studies. The compositions of minerals are used to describe the nature of magma and estimate the pressure and temperature at which the Moshirabad pluton was emplaced. Feldspar compositions are near the binary systems in which plagioclase compositions range from An5 to An53 and alkali‐feldspar compositions range from Or91 to Or97. Mafic minerals in the plutonic rocks are biotite and hornblende. Based on the composition of biotites and whole‐rock chemistry, the Moshirabad pluton formed from a calc‐alkaline magma. Amphiboles are calcic amphiboles (magnesio‐hornblende or edenite). Temperatures of crystallization, calculated with the hornblende–plagioclase thermometer, range 550–750°C. These temperatures indicate that plutonic rocks have undergone some retrogressive changes in their mineral compositions. Aluminum‐in‐hornblende geobarometry indicates that the Moshirabad pluton was emplaced at pressures of 2.3–6.0 kbar, equal to depths of 7–20 km, but with consideration of regional geology, lower pressures than the above pressure range are more probable. Alteration of amphiboles can be the reason for some overestimation of pressures.  相似文献   

4.
The 29.5 Ma Wah Wah Springs Formation which erupted from the Indian Peak Caldera has an estimated volume of > 3900 km3 making it one of the largest ignimbrites on earth. The magma was calc-alkaline, dacitic (68 wt. % SiO2) and phenocryst-rich (38 vol.%). Phenocrysts include plagioclase (An 47), magnesio-hornblende, Mg-biotite, quartz, Fe-Ti oxides, diopsidic-augite, and rare Ca-poor pyroxene, in order of decreasing abundance. Apatite, zircon and pyrrhotite occurs as inclusions within phenocrysts. Atmospheric glass losses (1040 km3) account for bulk-rock compositions that have SiO2 contents ranging from 63 to 67 wt.%. Glass compositions are high-silica rhyolite.Phenocrysts equilibrated at temperatures ranging from about 790 to 850°C and oxygen fugacities approximately 2.6 log units above the QFM buffer. Confining pressure estimates using the aluminum-in-hornblende geobarometer calibrated for calc-alkaline volcanic rocks suggest a mean pressure of 230±50 MPa corresponding to 7.5±1.5 km depth. These estimates are consistent with caldera formation accompanying emplacement.Crystal compositions for phenocrysts and mineral inclusions within phenocrysts are remarkably homogeneous throughout the outflow tuff, although minor zoning does occur. Given the dacitic composition of the magma, the weakly zoned phenocryst population cannot be modeled to produce the observed high-silica glass (melt) indicating open-system behavior for the magma. The high-silica rhyolite glass is interpreted to be an artifact of efficient magma mixing accompanying addition of highly evolved magma, or melt to intermediate composition magma. Mixing was followed by magma hybridization. Additional support for this hybridization model includes: (1) physically and chemically distinct populations of augite; (2) minor but unbiquitous resorbed plagioclase, biotite and hornblende phenocrysts; and (3) reverse zoning in some of the plagioclase euhedra within pumice lapilli.  相似文献   

5.
The Etendeka Formation of north-western Namibia consists of a sequence of interbedded quartz latites and tholeiitic basalts and forms part of the Karoo Igneous Province in southern Africa. The age of the Etendeka Formation is approximately 130–135 Ma. The quartz latites make up a significant proportion of the stratigraphic succession (<25% of the total stratigraphic thickness) and form as much as 60% of the outcrop area in the southern Etendeka. Apart from some systematic differences between pitchstones and devitrified quartz latite, largely explained by alteration processes, individual quartz latite units exhibit remarkably uniform compositions with no significant vertical or lateral variation. Geochemistry can be used as a primary criterion for the correlation of major quartz latite units over much of the southern Etendeka area enabling the reconstruction of the Etendeka Formation stratigraphy in this region. Individual quartz latite units occur as voluminous (400–2600 km3), widespread (up to 8800 km2), sheet-like deposits typically between 40 and 300 m thick. Each unit consists of basal, main and upper zones. The main zone generally constitutes over 70% of the thickness of the unit and typically consists of texturally featureless devitrified quartz latite. In contrast the basal and upper zones of the flow are characterised by flow banding, pitchstone lenses and breccia, with rare occurrences of pyroclastic textures. The quartz latites are sparsely porphyritic (<10% phenocrysts) with glassy or devitrified groundmass textures. The phenocrysts consist of plagioclase, pyroxene, titanomagnetite and rare ilmenite. Pyroxene geothermometry indicates high (1000–1100°C) temperatures of crystallisation which, coupled with the absence or primary hydrous phases, indicates that the quartz latites were relatively hot, H2O-undersaturated magmas. The quartz latites display features common to both rhyolite lavas and ignimbrites and are clearly the products of an unusual eruption style. The local preservation of pyroclastic textures and the broad areal extent of these units lead to the conclusion that the quartz latites are high-temperature rheomorphic ignimbrites (i.e. rheoignimbrites). A combination of high eruption temperature and relatively low viscosity helps to explain the often completely welded and homogeneous textures observed in most quartz latite outcrops in the Etendeka area.  相似文献   

6.
 The 1963 eruption of Gunung Agung produced 0.95 km3 dense rock equivalent (DRE) of olivine±hornblende-bearing, weakly phyric, basaltic andesite tephra and lava. Evidence for magma mixing in the eruptive products includes whole-rock compatible and incompatible trace element trends, reverse and complex compositional zoning of mineral phases, disequilibrium mineral assemblages, sieve-textured plagioclase phenocrysts, and augite rims on reversely zoned orthopyroxene. Basalt magma mixed with pre-existing andesite magma shortly before eruption to yield basaltic andesite with a temperature of 1040–1100  °C at an assumed pressure of 2 kb, f O2>NNO, and an average melt volatile content (H2O±CO2) of 4.3 wt.%. Magma-mixing end members may have provided some of the S and Cl emitted in the eruption. Glass inclusions in phenocrysts contain an average of 650 ppm S and 3130 ppm Cl as compared with 70 ppm and 2220 ppm, respectively, in the matrix glass. Maximum S and Cl contents of glass inclusions approach 1800 and 5000 ppm, respectively. Application of the petrologic method to products of the 1963 eruption for estimating volatile release yields of 2.5×1012 g (Mt) of SO2 and 3.4 Mt of Cl released from the 0.65 km3 of juvenile tephra which contributed to stratospheric injection of H2SO4 aerosols on 17 March and 16 May, when eruption column heights exceeded 20 km above sea level. An independent estimate of SO2 release from atmospheric aerosol loading (11–12 Mt) suggests that approximately 7 Mt of SO2 was injected into the stratosphere. The difference between the two estimates can be most readily accounted for by the partitioning of S, as well as some Cl, from the magma into a water-rich vapor phase which was released upon eruption. For other recent high-S-release eruptions of more evolved and oxidized magmas (El Chichón, Pinatubo), the petrologic method gives values two orders of magnitude less than independent estimates of SO2 emissions. Results from this study of the Agung 1963 magma and its volatile emissions, and from related studies on eruptions of more mafic magmas, suggest that SO2 emissions from eruptions of higher-S-solubility magma may be more reliably estimated by the petrologic method than may those from more-evolved magma eruptions. Received: 29 June 1994 / Accepted: 25 April 1996  相似文献   

7.
Gases trapped in lavas of three main flows of the Ardoukôba eruption (8 to 15 November, 1978) have been analysed by mass spectrometry. These analyses concern both plagioclase phenocrysts and microcrystalline mesostasis. Fluids are released between 500°C and 1200°C, and consist of H2O, CO2, CO, N2, SO2, HCl, H2, CH4 with traces of hydrocarbons and H2S. The total content is less than 0.3–0.4 wt. % of samples with about 0.1–0.15 wt % of H2O. No significant variation among the three flows is observed. Plagioclase phenocrysts are less abundant in fluids than the mesostasis (～2/3). The gases trapped in these phenocrysts are richer in CO and organic compounds, whereas mesostasis contain more H2O, CO2 and SO2. CO is likely produced by reduction of CO2 and H2O with carbon during either analyses or eruption itself, or is of primary origin. In the latter case, gas composition suggests an entrapment temperature of about 1200°C ± 75°C. Kinetic study of the water and carbon dioxide release allows to calculate the diffusion characteristics of these fluids. Water and carbon dioxide behave rather similarly. Plagioclase gives a single activation energy value (8 Kcal/mole), while mesostasis gives two values (8 Kcal/mole, 15 Kcal/mole). Diffusion coefficients at 20°C are estimated to fall in the range 10?13 · 10?12 cm2 · sec?1.  相似文献   

8.
The rhyodactic O’Leary Porphyry which forms the Pleistocene (0.233±0.37 m.y.) volcanic domes of O’Leary Peak and Darton Dome in the San Francisco Volcanic Field (northern Arizona, U.S.A.) contains sanidine phenocrysts with oligoclase mantles (rapakivi texture). Rapakivi texture occurs worldwide in silicic rocks of many ages and has been attributed to various igneous and metamorphic processes. The O’Leary Porphyry contains both mantled and unmantled sanidine (both are Or63–69 Ab30–36An1), oligoclase and quartz phenocrysts, labradorite (An53Ab45Or2) and kaersutite xenocrysts and andesite xenoliths. The compositional range of oligoclase is the same (An11–26Ab70–80Orr–10) for the rapakivi mantles, the oligoclase phenocrysts, and the oligoclase crystals poikilitic within sanidines. Most mantles are discontinuous. The sanidine appears to have been resorbed prior to mantling. Experimental melting studies on the O’Leary Prophyry show that, for a 15 wgt.% water system, plagioclase crystallized prior to sanidine and quartz crystallized last. The O’Leary Porphyry, although inhomogeneous, plots on a Q-Or-Ab-An diagram well within the plagioclase stability field. Poikilitic plagioclases within sanidines further support crystallization of plagioclase prior to sanidine in the O’Leary Porphyry. Exsolution of a ternary feldspar to form a plagioclase mantle is the most commonly accepted igneous theory of rapakivi texture formation but has been eliminated as the origin of the O’Leary Porphyry rapakivi. Petrologic models by Tuttle and Bowen and by Stewart are rejected for the O’Leary rapakivi because of inconsistencies with the O’Leary occurrences. Two theories are viable for the O’Leary rapakivi texture. First, is a decrease in water vapor pressure which would enlarge the plagioclase stability field possibility causing mantling of metastable sanidines. The second and preferred theory is that of an addition of sodium and calcium by basification (chemical assimilation without melting) of the xenoliths within the O’Leary Porphyry. This would move the bulk composition of the melt into the plagioclase field possibly resulting in crystallization of plagioclase on sanidine crystals. Diffusion of sodium and calcium from the xenoliths to sanidine would result in mantling only those crystals near to the xenoliths. Later, convection would result in distribution throughout the melt of rapakivi, unmantled sanidines, and xenolithic kaersutite as is seen in the porphyry. Basic xenoliths are extremely common in rapakivi-bearing rocks. Those within the O’Leary Porphyry are andesitic and show resorption, and in some areas of O’Leary Peak itself, have been drawn out into schlieren.  相似文献   

9.
Volcanism in the Taupo Volcanic Zone (TVZ) and the Kermadec arc-Havre Trough (KAHT) is related to westward subduction of the Pacific Plate beneath the Indo-Australian Plate. The tectonic setting of the TVZ is continental whereas in KAHT it is oceanic and in these two settings the relative volumes of basalt differ markedly. In TVZ, basalts form a minor proportion (< 1%) of a dominant rhyolite (97%)-andesite association while in KAHT, basalts and basaltic andesites are the major rock types. Neither the convergence rate between the Pacific and Indo-Australian Plates nor the extension rates in the back-arc region or the dip of the Pacific Plate Wadati-Benioff zone differ appreciably between the oceanic and continental segments. The distance between the volcanic front and the axis of the back-arc basin decreases from the Kermadec arc to TVZ and the distance between trench and volcanic front increases from around 200 km in the Kermadec arc to 280 km in TVZ. These factors may prove significant in determining the extent to which arc and backarc volcanism in subduction settings are coupled.All basalts from the Kermadec arc are porphyritic (up to 60% phenocrysts) with assemblages generally dominated by plagioclase but with olivine, clinopyroxene and orthopyroxene. A single dredge sample from the Havre Trough back arc contains olivine and plagioclase microphenocrysts in glassy pillow rind and is mildly alkaline (< 1% normative nepheline) contrasting with the tholeiitic nature of the other basalts. Basalts from the TVZ contain phenocryst assemblages of olivine + plagioclase ± clinopyroxene; orthopyroxene phenocrysts occur only in the most evolved basalts and basaltic andesites from both TVZ and the Kermadec Arc.Sparsely porphyritic primitive compositions (Mg/(Mg+Fe2) > 70) are high in Al2O3 (>16.5%), and project in the olivine volume of the basalt tetrahedron. They contain olivine (Fo87) phenocrysts and plagioclase (> An60) microphenocrysts. These magmas have ratios of CaO/Al2O3, A12O3/TiO2 and CaO/TiO2 in the range of MORB and MORB picrites and can evolve to the low-pressure MORB cotectic by crystallisation of olivine±plagiociase. Such rocks may be the parents of other magmas whose evolutionary pathways are complicated by interaction of crystal fractionation, crystal accumulation and mixing processes and the filtering action of crust of variable density and thickness. The interplay of these processes likely accounts for the scatter of data about the cotectic. More evolved rocks from both TVZ and KAHT contain clinopyroxene and orthopyroxene phenocrysts and their compositions merge with basaltic andesites and andesites. Stepwise least-squares modelling using phenocryst assemblages in proportions observed in the rocks suggest that crystal fractionation and accumulation processes can account for much of the diversity observed in the major-element compositions of all lavas.We conclude that the parental basaltic magmas for volcanism in the TVZ and KAHT segments are similar thereby implying grossly similar source mineralogy. We attribute the diversity to secondary processes influencing liquids as they ascended through complex plumbing systems in the sub arc mantle and cross.  相似文献   

10.
A mixture containing equal amounts of forsterite and grossularite by weight (Fo50Gr50) has been studied at temperatures between 750 and 1400°C under pressures ranging from 6 to 25 kbar in presence of excess water. The assemblages noted under low pressure (<8 kbar) are as follows: Diopsidess+forsteritess+monticellitess+vapor and Diopsidess+forsteritess+monticellitess+liquid+vapor. (ss denotes solid solution) Under intermediate pressures between 8 and 24 kbar following assemblages were noted in the order of increasing temperature: Diopsidess+forsteritess+spinel+vapor, Diopsidess+forsteritess+spinel+liquid+vapor, Diopsidess+forsteritess+liquid+vapor, and Forsteritess+liquid+vapor. At pressures above 24 kbar the assemblages are as follows: Diopsidess+forsteritess+garnet+vapor, Diopsidess+forsteritess+garnet+liquid+vapor, Diopsidess+forsteritess+liquid+vapor, and Forsteritess+liquid+vapor. Electron microprobe analyses of diopside and forsterite crystallized at 1050°C and 23 kbar, show that the former contains 6 to 6.5 wt % of Al2O3 as solid solution whereas the latter incorporates 1.3 wt % of monticellite in solid solution. The monticellite content of forsterite increases at low pressures at a given temperature to about 6 wt % at 1050°C and 6 kbar. The study indicates that forsteritic olivine does not coexist with pure grossularite in the studied temperature and pressure ranges, although the former is in equilibrium with pyrope-rich garnet, containing 23 mole % grossularite. The study supports the conclusion ofWerner andLuth (1973) that the solubility of monticellite in forsterite decreases with increasing pressure at a given temperature. The results of the investigation are also in agreement with the findings ofKushiro andYoder (1966), who noted that spinel peridotites found in folded belts and in alkalic basalts are produced under intermediate pressures, whereas garnet peridotite xenoliths found in kimberlite and in orogenic belts are formed at high pressures.  相似文献   

11.
The Angra dos Reis meteorite fell in 1869 and is a unique achondrite. It is an ultramafic igneous rock, pyroxenite, with 93% fassaite pyroxene which has 15.7% Ca-Tschermak's molecule, plus calcic olivine (Fo53.1; 1.3% CaO), green hercynitic spinel, whitlockite (merrillite), metallic Ni-Fe, troilite, as well as magnesian kirschsteinite (Ks62.3Mo37.7), within olivine grains, and celsian (Cs90.2An7.7Ab1.7Or0.4) which are phases reported in a meteorite for the first time, and plagioclase (An86.0), baddeleyite, titanian magnetite (TiO2, 21.9%), and terrestrial hydrous iron oxide which are phases reported for the first time in this meteorite. Petrofabric analysis shows that fassaite has a preferred orientation and lineation which is interpreted as being due to cumulus processes, possibly the effect of post-depositional magmatic current flow or laminar flow of a crystalline mush. The mineral chemistry indicates crystallization from a highly silica-undersaturated melt at low pressure. Since the meteorite formed as a cumulate, pyroxene crystals may have gravitationally settled from a melt which crystallized melilite first. Plagioclase would be unstable in such a highly undersaturated melt, and feldspathoids would be rare or absent due to the very low alkali contents of the melt. The presence of rare grains of plagioclase and celsian may be the result of late-stage crystallization of residual liquids in local segregations. Thus, the Eu anomaly in Angra dos Reis may be the result of pyroxene separation from a melt which crystallized melilite earlier, rather than plagioclase as previously suggested.  相似文献   

12.
Abstract On the island of Mustique, fresh and propylitized olivine–plagioclase–clinopyroxene basalt, plagioclase–clinopyroxene–orthopyroxene and plagioclase–clinopyroxene–amphibole andesite lavas and minor intrusions are interbedded with Oligocene pyroclastic and epiclastic rocks. Chemical data show that two isotopically identical, but chemically different, suites of lava are present: (i) the OPXS (87Sr/86Sr 0.70403–0.70454; 143Nd/144Nd 0.512952–0.512986; δ18Ocpx 5.49 and 5.61), comprising basalts and orthopyroxene‐bearing andesites; and (ii) the AMPHS (87Sr/86Sr 0.70401–0.70457; 143Nd/144Nd 0.512981–0.513037; δ18Ocpx 5.54), made up of basalts and amphibole‐bearing andesites. The OPXS has higher contents of TiO2, P2O5, light rare earth elements, Sm, Pb, Th, U, Zr, Y and Nb, and higher La/Yb ratios than the AMPHS. The isotopic data suggest that both suites formed from melts derived from the same subduction‐modified depleted mantle source as the volcanic rocks of nearby St Vincent and Bequia, and the northern islands of the Lesser Antilles Arc. The immobile trace element contents, and La/Yb ratios, of the OPXS are indicative of ～10% partial melting of the source, whereas those of the AMPHS are indicative of ～25% partial melting. The within‐suite chemical variation of the OPXS is consistent with ～45% fractional crystallization of its intratelluric mineral assemblages, and that of the AMPHS is consistent with the removal of ～65% of its intratelluric assemblages. Experimental evidence suggests that both suites of basalt crystallized at pressures <8 kbar from melts containing 1–2 wt% water. After extensive fractional crystallization, the andesites crystallized at pressures between approximately 5 and 2 kbar. The OPXS magmas appear to have lost more of their water content than the AMPHS magmas. Thus, the OPXS andesites formed from melts with an estimated water content of 2–3 wt%, whereas the AMPHS andesites formed from melts containing at least 4.5 wt% water.  相似文献   

13.
 Measurements of CO2 fluxes from open-vent volcanos are rare, yet may offer special capabilities for monitoring volcanos and forecasting activity. The measured fluxes of CO2 and SO2 from Mount St. Helens decreased from July through November 1980, but the record includes variations of CO2/SO2 in the emitted gas and episodes of greatly increased fluxes of CO2. We propose that the CO2 flux variations reflect two gas components: (a) a component whose flux decreased in proportion to 1/ √t with a CO2/SO2 mass ratio of 1.7, and (b) a residual flux of CO2 consisting of short-lived, large peaks with a CO2/SO2 mass ratio of 15. We propose two hypotheses: (a) the 1/ √t dependence was generated by crystallization in a deep magma body at rates governed by diffusion-limited heat transfer, and (b) the gas component with the higher CO2/SO2 was released from ascending magma, which replenished the same magma body. The separation of the total CO2 flux into contributions from known processes permits quantitative inferences about the replenishment and crystallization rates of open-system magma bodies beneath volcanos. The flux separations obtained by using two gas sources with distinct CO2/SO2 ratios and a peak minus background approach to obtain the CO2 contributions from an intermittent source and a continuously emitting source are similar. The flux separation results support the hypothesis that the second component was generated by episodic magma ascent and replenishment of the magma body. The diffusion-limited crystallization hypothesis is supported by the decay of minimum CO2 and SO2 fluxes with 1/ √t after 1 July 1980. We infer that the magma body at Mount St. Helens was replenished at an average rate (2.8×106 m3 d–1) which varied by less than 5% during July, August, and September 1980. The magma body volume (2.4–3.0 km3) in early 1982 was estimated by integrating a crystallization rate function inferred from CO2 fluxes to maximum times (20±4 years) estimated from the increase of sample crystallinity with time. These new volcanic gas flux separation methods and the existence of relations among the CO2 flux, crystallization rates, and magma body replenishment rates yield new information about the dynamics of an open-vent, replenished magma body. Received: 15 February 1995 / Accepted: 30 March 1996  相似文献   

14.
The properties of the seismic low-velocity zone are consistent with incipient melting of mantle peridotite. Vapor-absent melting of amphibole-peridotite has been used to model the low-velocity zone, but evidence that CO2 exists in the upper mantle indicates that peridotite-CO2-H2O would be a better model. The divariant solidus surface for peridodite-CO2-H2O is traversed by a series of univariant lines marking the intersections of divariant subsolidus reactions involving dolomite or magnesite, amphibole, or phlogopite (other hydrous minerals are neglected in this treatment), or combinations of these. The vapor phase compositions are buffered to specific values, which limits the range of vapor compositions that can coexist with peridotite at various pressures. Below about 30 kbar, the vapor phase is buffered by the melting of amphibole-peridotite, with composition ranging from H2O to high CO2/H2O. Above about 25 kbar, the vapor phase is buffered by the melting of dolomite-peridotite, with composition ranging from CO2 to high H2O/CO2 at pressures above 30 kbar. The buffered curve for phlogopite-peridotite intersects the dolomite-peridotite curve, generating another line for phlogopite-dolomite-peridotite; the strong buffering capacity of dolomite forces the vapor on this line to high H2O/CO2. Near the buffered curve for the solidus of partly carbonated peridotite there is a temperature maximum on the peridotite-vapor solidus surface. On the CO2 side of the maximum, above 26 kbar, CO2/H2O is greater in liquid than in vapor; on the H2O side of this maximum, and at all pressures below 26 kbar, CO2/H2O is greater in vapor than in liquid. The suboccanic low-velocity zone is caused by incipient melting of amphibole-peridotite in the presence of vapor with high CO2/H2O, with generation of forsterite-normative liquid. The subcontinental low-velocity zone, where present, is probably caused by incipient melting of dolomite-peridotite, or phlogopite-dolomite-peridotite, either with H2O-rich vapor or without vapor, with the generation of CO2-rich, alkalic, SiO2-poor liquid (larnite-normative) that in extreme conditions may be carbonatitic.  相似文献   

15.
CO2 has been investigated up to 514 kbar at23 ± 2°C by both optical and in situ X-ray diffraction studies using a diamond-anvil pressure cell. CO2 solidifies in an unknown structure in the pressure range 5 to 23 kbar, and transforms to ordinary dry-ice structure above 23 kbar at room temperature. Isothermal compression data for dry ice have been obtained above about 24 kbar. These appear to be the first data at room temperature known in the literature. The data fitted to the Birch equation of state yieldK0 = 29.3 ± 1.0kbar andK0′ = 7.8 assuming the volume of the hypothetical dry ice at zero-pressure and room temperature is 31.4 ± 0.2 cm3/mole. The isothermal bulk modulus(K0) thus derived is consistent with the compression data and compressibilities for dry ice obtained at low temperatures using dilatometry and ultrasonic techniques, respectively, reported in the literature. By comparing shock-wave data for relevant materials, it is suggested that CO2 is not likely to transform to one of the crystalline forms of SiO2 which is otherwise expected from empirical grounds, but may instead decompose into C (diamond) + O2, at high pressures.  相似文献   

16.
Minerals formed during magma crystallization trap droplets of melt that are preserved as primary or secondary inclusions. Depending on the rate of cooling, the droplets may solidify as glass, or crystallize. Inclusions may contain one or more bubbles, or none. When inclusions are heated the glass or crystalline material are melted and the inclusion expands, the size of bubbles diminishes, and homogenization of the inclusion occurs. It is possible to observe these transformations by means of high-temperature cameras which permit visual observations to 1600°C and above. The possibility of using the homogenization of inclusions to determine the temperature of formation of the host mineral has been demonstrated experimentally, using inclusions in artificial diopside formed at 1300 ± 10°. Melt inclusions in phenocrysts from nepheline basalt, fergusite porphyry, and tephrite were investigated. In the leucite-bearing rocks leucite crystallized at 1600° or above, and clinopyroxene in the range 1380–1250°. The central part of olivines in nepheline basalt formed at 1290–1270° and the peripheral zones at 1160–1120°; nepheline formed at 1290–1250°; the central part of pyroxenes at 1280–1250° and the peripheral zones at 1160–1120°. These temperatures suggest almost dry magma. Gas from the bubbles of individual inclusions has been analyzed. The predominant gaseous component of the early crystallization stage of the nepheline basalt and fergusite porphry was CO2, H2S, SO2, NH., HCl, HF, and H. comprise less than 5 volume percent except in olivine of olivine basalt in which the total content of these gases was on average 6.22 volume percent, and in leucite of fergusite porphyry in which H2 was on average 12.7 volume percent. The main gas component in the crystallization of the leucite tephrite were nitrogen and rare gases. Liquid hydrocarbons in the secondary inclusions in pyroxene from nepheline basalt can be accounted for by their assimilation by the magma from enclosing rocks during its rise.  相似文献   

17.
The Niyasar plutonic complex, one of the Cenozoic magmatic assemblages in the Urumieh‐Dokhtar magmatic belt, was the subject of detailed petrographic and mineralogical investigations. The Niyasar magmatic complex is composed of Eocene to Oligocene mafic rocks and Miocene granitoids. Eleven samples, representing the major rock units in the Niyasar magmatic complex and contact aureole were chosen for mineral chemical studies and for estimation of the pressure, temperature, and oxygen fugacity conditions of mineral crystallization during emplacement of various magmatic bodies. The analyzed samples are composed of varying proportions of quartz, plagioclase, K‐feldspar, hornblende, biotite, titanite, magnetite, apatite, zircon, garnet, and clinopyroxene. Application of the Al‐in‐hornblende barometer indicates pressures of around 0.2 to 0.4 kbar for the Eocene–Oligocene mafic bodies and around 0.5 to 1.7 kbar for the Miocene granitoids. Hornblende‐plagioclase thermometry yields relatively low temperatures (661–780 °C), which probably reflect late stage re‐equilibration of these minerals. The assemblage titanite–magnetite–quartz as well as hornblende composition were used to constrain the oxygen fugacity and H2O content during the crystallization of the parent magmas in the Miocene plutons. The results show that the Miocene granitoids crystallized from magmas with relatively high oxygen fugacity and high H2O content (~5 wt% H2O). The Miocene granitoids show similar range of oxygen fugacity, H2O contents and mineral chemical compositions, which indicate a common source for their magmas. Although the crystallization pressures of the Miocene plutons discriminate various categories of plutonic bodies emplaced at depths of about 5.7–6.5 km (Marfioun pluton), about 4.2 km (Ghalhar pluton) and 1.9–2.3 km (Poudalg pluton), they were later uplifted to the same level by vertical displacement of faults. The emplacement depths of the Niyasar plutons suggest that the central part of the Urumieh‐Dokhtar magmatic belt has experienced an uplift rate of ca. 0.25–0.4 mm/yr from the Miocene onwards.  相似文献   

18.
Magma plumbing system of the 2000 eruption of Miyakejima Volcano, Japan   总被引：1，自引：0，他引：1  
During the 2000 eruption at Miyakejima Volcano, two magmas with different compositions erupted successively from different craters. Magma erupted as spatter from the submarine craters on 27 June is aphyric basaltic andesite (<5 vol% phenocrysts, 51.4–52.2 wt% SiO2), whereas magma issued as volcanic bombs from the summit caldera on 18 August is plagioclase-phyric basalt (20 vol% phenocrysts, 50.8–51.3 wt% SiO2). The submarine spatter contains two types of crystal-clots, A-type and A-type (andesitic type). The phenocryst assemblages (plagioclase, pyroxenes and magnetite) and compositions of clinopyroxene in these clots are nearly the same, but only A-type clots contain Ca-poor plagioclase (An < 70). We consider that the A-type clots could have crystallized from a more differentiated andesitic magma than the A-type clots, because FeO*/MgO is not strongly influenced during shallow andesitic differentiation. The summit bombs contain only B-type (basaltic type) crystal-clots of Ca-rich plagioclase, olivine and clinopyroxene. The A-type and B-type clots have often coexisted in Miyakejima lavas of the period 1469–1983, suggesting that the magma storage system consists of independent batches of andesitic and basaltic magmas. According to the temporal variations of mineral compositions in crystal-clots, the andesitic magma became less evolved, and the basaltic magma more evolved, over the past 500 years. We conclude that gradually differentiating basaltic magma has been repeatedly injected into the shallower andesitic magma over this period, causing the andesitic magma to become less evolved with time. The mineral chemistries in crystal-clots of the submarine spatter and 18 August summit bombs of the 2000 eruption fall on the evolution trends of the A-type and B-type clots respectively, suggesting that the shallow andesitic and deeper basaltic magmas existing since 1469 had successively erupted from different craters. The 2000 summit collapse occurred due to drainage of the andesitic magma from the shallower chamber; as the collapse occurred, it may have caused disruption of crustal cumulates which then contaminated the ascending, deeper basalt. Thus, porphyritic basaltic magma could erupt alone without mixing with the andesitic magma from the summit caldera. The historical magma plumbing system of Miyakejima was probably destroyed during the 2000 eruption, and a new one may now form.Editorial responsibility: S Nakada, T Druitt  相似文献   

19.
Mount Erebus, Antarctica, is a large (3794 m) alkaline open-conduit stratovolcano that hosts a vigorously convecting and persistently degassing lake of anorthoclase phonolite magma. The composition of the lake was investigated by analyzing glass and mineral compositions in lava bombs erupted between 1972 and 2004. Matrix glass, titanomagnetite, olivine, clinopyroxene, and fluor-apatite compositions are invariant and show that the magmatic temperature (∼ 1000°C) and oxygen fugacity (ΔlogFMQ = − 0.9) have been stable. Large temperature variations at the lake surface (~ 400–500°C) are not reflected in mineral compositions. Anorthoclase phenocrysts up to 10 cm in length feature a restricted compositional range (An10.3–22.9Ab62.8–68.1Or11.4–27.2) with complex textural and compositional zoning. Anorthoclase textures and compositions indicate crystallization occurs at low degrees of effective undercooling. We propose shallow water exsolution causes crystallization and shallow convection cycles the anorthoclase crystals through many episodes of growth resulting in their exceptional size. Minor variations in eruptive activity from 1972 to 2004 are decoupled from magma compositions. The variations probably relate to changes in conduit geometry within the volcano and/or variable input of CO2-rich volatiles into the upper-level magma chamber from deeper in the system.  相似文献   

20.
Phase assemblages for five selected compositions in the system CaSiO3-Al2O3 have been investigated in the pressure range 100–300 kbar and at about 1000°C in a diamond-anvil press coupled with laser heating. At pressures below about 250 kbar, the assemblage of grossularite plus corundum is stable for compositions containing more than 25 mole% Al2O3. Above about 250 kbar, phase assemblages for the latter compositions are truncated by those in the join CaAl2O4-SiO2. Garnet solid solutions are stable between about 10 and 25 mole% Al2O3. Grossularite transforms to a new tetragonal form at pressures greater than about 250 kbar, but the stability field for the garnet solid solutions extends to pressures up to about 300 kbar. The perovskite modification appears to be stable at pressures above about 150 kbar, but is probably limited to nearly pure CaSiO3 composition. Phase behaviour for calcium-bearing silicates or aluminosilicates in the lower mantle are apparently more complicated than was suggested earlier.  相似文献   

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